Ignite Creation Date:
2024-10-26 @ 3:38 PM
Last Modification Date:
2024-10-26 @ 3:38 PM
Study NCT ID:
NCT06558929
Status:
NOT_YET_RECRUITING
Last Update Posted:
None
First Post:
2024-08-13
Brief Title:
Evaluating the Effectiveness of Intervention Based on the Model of Occupational Harmony in Patients With CRSWD
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Evaluating the Effectiveness of Intervention Based on the Model of Occupational Harmony in Patients With Circadian Rhythm Sleep-Wake Disorders CRSWD
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-08
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The goal of this clinical trial is to learn the effectiveness of an intervention based on the Model of Occupational Harmony MOHar in treating patients with circadian rhythm sleep-wake disorders CRSWD The main questions it aims to answer are
Does intervention based on the MOHar can improve sleep quality in patients with CRSWD
Does intervention based on the MOHar can improve the quality of life in patients with CRSWD
Researchers will compare intervention based on the MOHar to conventional treatment to see if the intervention works to treat CRSWD
Participants will
Participate in an occupational therapy program for 6 weeks including group therapy individual treatment and daily occupational tasks
Complete questionnaires at 1 3 and 6 months after the program for follow-up
Does intervention based on the MOHar can improve sleep quality in patients with CRSWD
Does intervention based on the MOHar can improve the quality of life in patients with CRSWD
Researchers will compare intervention based on the MOHar to conventional treatment to see if the intervention works to treat CRSWD
Participants will
Participate in an occupational therapy program for 6 weeks including group therapy individual treatment and daily occupational tasks
Complete questionnaires at 1 3 and 6 months after the program for follow-up
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None